Evidence map›Paper›PMID 40603866›Full record

ArticleNature communications2025

Uncovering causal gene-tissue pairs and variants through a multivariate TWAS controlling for infinitesimal effects.

Yihe Yang, Noah Lorincz-Comi, Xiaofeng Zhu

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Yihe YangDepartment of Population and Quantitative Health Sciences, Case Western Reserve University School of Medicine, Cleveland, OH, USA.ORCID http://orcid.org/0000-0001-6563-3579
Noah Lorincz-ComiDepartment of Population and Quantitative Health Sciences, Case Western Reserve University School of Medicine, Cleveland, OH, USA.ORCID http://orcid.org/0000-0002-0517-2499
Xiaofeng ZhuDepartment of Population and Quantitative Health Sciences, Case Western Reserve University School of Medicine, Cleveland, OH, USA. xxz10@case.edu.ORCID http://orcid.org/0000-0003-0037-411X

Funding

Genome-Wide Association Analysis in Essential Hypertension (FEHGAS study)R01HL086694 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ARAVINDA CHAKRAVARTI · 2007 to 2026
$21.2M
Statistical Analysis of Large Genomic Data SetsR01HG011052 · NHGRI · CASE WESTERN RESERVE UNIVERSITY · PI XIAOFENG ZHU · 2020 to 2026
$3.3M
NHGRI NIH HHS R01 HG011052NHLBI NIH HHS R01 HL086694U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL086694U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) HG011052
6 · The paper itself

Abstract

Transcriptome-wide association studies (TWAS) are commonly used to prioritize causal genes underlying associations found in genome-wide association studies (GWAS) and have been extended to identify causal genes through multivariate TWAS methods. However, recent studies have shown that widespread infinitesimal effects due to polygenicity can impair the performance of these methods. In this report, we introduce a multivariate TWAS method named tissue-gene pairs, direct causal variants, and infinitesimal effects selector (TGVIS) to identify tissue-specific causal genes and direct causal variants while accounting for infinitesimal effects. In simulations, TGVIS maintains an accurate prioritization of causal gene-tissue pairs and variants and demonstrates comparable or superior power to existing approaches, regardless of the presence of infinitesimal effects. In the real data analysis of GWAS summary data of 45 cardiometabolic traits and expression/splicing quantitative trait loci from 31 tissues, TGVIS is able to improve causal gene prioritization and identifies novel genes that were missed by conventional TWAS.

Indexed as

Genome-Wide Association StudyTranscriptomeComputer SimulationGene Expression ProfilingHumansModels, GeneticMultifactorial InheritanceOrgan SpecificityPolymorphism, Single NucleotideQuantitative Trait Loci

Identifiers

PMID40603866
PMCPMC12223092

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.